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2. Amniotic fluid secretor typing: validation for use in prenatal prediction of myotonic dystrophy. Teichler-Zallen D; Doherty RA Clin Genet; 1980 Oct; 18(4):257-67. PubMed ID: 6449321 [TBL] [Abstract][Full Text] [Related]
3. Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion. Renwick JH; Bundey SE; Ferguson-Smith MA; Izatt MM J Med Genet; 1971 Dec; 8(4):407-16. PubMed ID: 5149523 [No Abstract] [Full Text] [Related]
4. The secretor locus as a marker for prenatal prediction of myotonic dystrophy (DM). Greiner J; Spengler DH; Krüger J; Tariverdian G Hum Genet; 1988 Apr; 78(4):330-2. PubMed ID: 3162894 [TBL] [Abstract][Full Text] [Related]
5. An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy. Renwick JH; Bolling DR J Med Genet; 1971 Dec; 8(4):399-406. PubMed ID: 5149522 [No Abstract] [Full Text] [Related]
8. Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studies. Speer MC; Pericak-Vance MA; Yamaoka L; Hung WY; Ashley A; Stajich JM; Roses AD Neurology; 1990 Apr; 40(4):671-6. PubMed ID: 2320244 [TBL] [Abstract][Full Text] [Related]
9. Lewis and ABH substances in amniotic fluid obtained by amniocentesis. Arcilla MB; Sturgeon P Pediatr Res; 1972 Dec; 6(12):853-8. PubMed ID: 4643534 [No Abstract] [Full Text] [Related]
10. [Neonatal Steinert's disease: apropos of 2 cases in 2 successive generations]. Bétrémieux P; Blin-Jezequel E; Lefrançois C; Le Marec B J Genet Hum; 1985 Jan; 33(1):21-30. PubMed ID: 3856628 [TBL] [Abstract][Full Text] [Related]
11. The secretor status of the foetus. Gibson SL; Ferguson-Smith MA Clin Genet; 1980 Aug; 18(2):97-102. PubMed ID: 6449320 [TBL] [Abstract][Full Text] [Related]
13. Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy. Amiel J; Raclin V; Jouannic JM; Morichon N; Hoffman-Radvanyi H; Dommergues M; Feingold J; Munnich A; Bonnefont JP J Med Genet; 2001 Dec; 38(12):850-2. PubMed ID: 11768387 [No Abstract] [Full Text] [Related]
14. Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family. Lucotte G; Berriche S; David F; Mariotti M; Turpin JC Genet Couns; 1994; 5(2):171-4. PubMed ID: 7917127 [TBL] [Abstract][Full Text] [Related]
16. [Amniocentesis and prenatal cytogenetic diagnosis (author's transl)]. Grote W; von der Crabben H Dtsch Med Wochenschr; 1974 Jul; 99(29):1532-5. PubMed ID: 4277124 [No Abstract] [Full Text] [Related]
17. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review. Geifman-Holtzman O; Fay K Am J Med Genet; 1998 Jul; 78(3):250-3. PubMed ID: 9677060 [TBL] [Abstract][Full Text] [Related]
18. Reproductive counselling for women with myotonic dystrophy. Magee AC; Hughes AE; Kidd A; Lopez De Munain A; Cobo AM; Kelly K; Dean J; Nevin NC J Med Genet; 2002 Mar; 39(3):E15. PubMed ID: 11897835 [No Abstract] [Full Text] [Related]
19. Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy. Myring J; Meredith AL; Harley HG; Kohn G; Norbury G; Harper PS; Shaw DJ J Med Genet; 1992 Nov; 29(11):785-8. PubMed ID: 1453427 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis in myotonic dystrophy type 1. Thirteen years of experience: implications for reproductive counselling in DM1 families. Martorell L; Cobo AM; Baiget M; Naudó M; Poza JJ; Parra J Prenat Diagn; 2007 Jan; 27(1):68-72. PubMed ID: 17154336 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]